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RESISTICK SOLID LAPAROSCOPIC ELECTRODES

K971621 Class II Traditional
Decision Date
1997-06-20
Sponsor / Applicant
Aaron Medical Industries

Technical Specification

510(k) Submission ID K971621
Product Code KNF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4160
Decision Date 1997-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESISTICK SOLID LAPAROSCOPIC ELECTRODES received FDA 510(k) clearance under submission number K971621, sponsored by Aaron Medical Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1997-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code KNF and 21 CFR 884.4160, within the Obstetrics/Gynecology review panel as a Class II device.